Institute of Cellular Medicine, Newcastle University and Freeman Hospital, Sir William Leech Research Centre, Respiratory Department, Newcastle upon Tyne, UK
Nuffield Department of Medicine, University of Oxford, Oxford, UK.
Eur Respir J. 2015 Oct;46(4):1021-32. doi: 10.1183/13993003.00148-2015. Epub 2015 Sep 4.
This randomised double-blind placebo-controlled parallel-group multicentre phase IIa study evaluated the effect of the CXCR2 antagonist AZD5069 on sputum neutrophil counts in adults with bronchiectasis.Patients were randomised 1:1 to receive AZD5069 80 mg or placebo orally twice daily for 28 days. Assessments included blood cell counts, inflammatory markers in blood, morning spontaneous sputum, lung function, safety and tolerability and patients completed daily BronkoTest diary cards. The primary outcome measure was the change in absolute sputum neutrophil count.Of 52 randomised patients, 45 completed treatment, 20 (76.9%) out of 26 receiving AZD5069 and 25 (96.2%) out of 26 receiving placebo. AZD5069 reduced the absolute neutrophil cell count in morning sputum by 69% versus placebo (p=0.004); percentage sputum neutrophil count was reduced by 36% (p=0.008). The number of infections/exacerbations was similar with AZD5069 and placebo (nine versus eight), but these led to more study discontinuations with AZD5069 (four versus zero). Sputum interleukin (IL)-6 and growth-regulated oncogene (GRO)-α and serum GRO-α, IL-1ß and IL-8 levels increased with AZD5069 versus placebo (all p<0.001), while serum high-sensitivity C-reactive protein levels did not change. AZD5069 was well tolerated.AZD5069 markedly reduced absolute sputum neutrophil counts in bronchiectasis patients, although this was not associated with improvements in clinical outcomes in this exploratory study.
这项随机、双盲、安慰剂对照、平行分组、多中心的 IIa 期研究评估了 CXCR2 拮抗剂 AZD5069 对支气管扩张症患者痰中性粒细胞计数的影响。患者按 1:1 随机分为接受 AZD5069 80mg 或安慰剂口服,每天两次,共 28 天。评估包括血细胞计数、血液中的炎症标志物、清晨自发性痰、肺功能、安全性和耐受性,患者每天填写 BronkoTest 日记卡。主要观察指标是痰中性粒细胞绝对计数的变化。在 52 名随机患者中,45 名完成了治疗,26 名接受 AZD5069 治疗的患者中有 20 名(76.9%),26 名接受安慰剂治疗的患者中有 25 名(96.2%)完成了治疗。与安慰剂相比,AZD5069 使清晨痰中的中性粒细胞绝对计数减少 69%(p=0.004);痰中性粒细胞百分比减少 36%(p=0.008)。AZD5069 与安慰剂的感染/加重次数相似(9 次对 8 次),但 AZD5069 导致更多的研究中止(4 次对 0 次)。与安慰剂相比,AZD5069 使血清白细胞介素(IL)-6 和生长调节致癌基因(GRO)-α以及血清 GRO-α、IL-1β和 IL-8 水平升高(均 p<0.001),而血清高敏 C 反应蛋白水平没有变化。AZD5069 耐受良好。AZD5069 显著降低了支气管扩张症患者的痰中性粒细胞绝对计数,但在这项探索性研究中,这与临床结局的改善无关。